b3galnt2
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  • Official Full Name
  • beta-1,3-N-acetylgalactosaminyltransferase 2
  • Synonyms
  • B3GALNT2; beta-1,3-N-acetylgalactosaminyltransferase 2; UDP GalNAc:betaGlcNAc beta 1,3 galactosaminyltransferase, polypeptide 2; UDP-GalNAc:beta-1,3-N-acetylgalactosaminyltransferase 2; MGC39558; beta-1,3-GalNAc-T2; beta-1,3-galactosaminyltransferase 2; b
Cat.#:B3GALNT2-003HTag:GST
Source (Host):Wheat GermSpecies:Human
Product nameRecombinant Human B3GALNT2 protein, GST-tagged
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Cat.#:B3GALNT2-10094HTag:His
Source (Host):E. coliSpecies:Human
Product nameRecombinant Human B3GALNT2, His-tagged
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Cat.#:B3GALNT2-2230MTag:His
Source (Host):Mammalian CellsSpecies:Mouse
Product nameRecombinant Mouse B3GALNT2 Protein
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Cat.#:B3GALNT2-2849ZTag:His
Source (Host):Mammalian CellsSpecies:Zebrafish
Product nameRecombinant Zebrafish B3GALNT2
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Cat.#:B3GALNT2-8550HCLTag:N/A
Source (Host):Species:Human
Product nameRecombinant Human B3GALNT2 293 Cell Lysate
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Protein Function

B3GALNT2 has several biochemical functions, for example, acetylgalactosaminyltransferase activity, acetylglucosaminyltransferase activity, galactosyltransferase activity. Some of the functions are cooperated with other proteins, some of the functions could acted by B3GALNT2 itself. We selected most functions B3GALNT2 had, and list some proteins which have the same functions with B3GALNT2. You can find most of the proteins on our site.
Function
Related Protein
Function acetylgalactosaminyltransferase activity
Related Protein B4GALNT3; DPY19L4; POMGNT2; GLT8D1; B3GALNT2; CHPF2; UGGT1; GTDC2; CSGALNACT1; PIGB
Function acetylglucosaminyltransferase activity
Related Protein C3orf39; POMGNT2; POC1BL; XYLT1; MGAT1B; PIGB; MGAT1A; B3GNTL1; GTDC2; GALNT18A
Function galactosyltransferase activity
Related Protein A4GALT; B3GNT3; B3GNT2A; GALNTL4; B3GNT2; B3GNT9-PS; GALNT18A; POMGNT2; B3GALT6; B3GNT2B

B3GALNT2 Related Articles

Hedberg, C; Oldfors, A; et al. B3GALNT2 is a gene associated with congenital muscular dystrophy with brain malformations. EUROPEAN JOURNAL OF HUMAN GENETICS 22:707-710(2014).
Stevens, E; Carss, KJ; et al. Mutations in B3GALNT2 Cause Congenital Muscular Dystrophy and Hypoglycosylation of alpha-Dystroglycan. AMERICAN JOURNAL OF HUMAN GENETICS 92:354-365(2013).